HGVS | Genome Assembly |
---|---|
NC_000010.11:g.97611574G>C , CM000672.2:g.97611574G>C | GRCh38 |
NC_000010.10:g.99371331G>C , CM000672.1:g.99371331G>C | GRCh37 |
NC_000010.9:g.99361321G>C | NCBI36 |
NG_027922.1:g.32230G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370646.9:c.899G>C MANE Select | ENSP00000359680.4:p.Gly300Ala | |
ENST00000370646.8:c.899G>C | ENSP00000359680.4:p.Gly300Ala | |
ENST00000370647.8:c.410G>C | ENSP00000359681.4:p.Gly137Ala | |
ENST00000370649.3:c.345+9584G>C | ENSP00000359683.3:n.345+9584G>C | |
NM_001134670.1:c.410G>C | NP_001128142.1:p.Gly137Ala | |
NM_138413.3:c.899G>C | NP_612422.2:p.Gly300Ala | |
NM_138413.4:c.899G>C MANE Select | NP_612422.2:p.Gly300Ala | |
NM_001134670.2:c.410G>C | NP_001128142.1:p.Gly137Ala |